QA Associate II/III

Astrix; California (MO); On-site; USD 48,216 - 68,880; Full time

Benefits offered by this job

Medical insurance

401(k)

Vision insurance

Job summary

A biotech staffing agency is seeking a QA Associate II/III to support quality operations within a manufacturing facility. The role ensures compliance with cGMP requirements and involves reviewing GMP documents, supporting product release, and providing QA oversight. Ideal candidates have a Bachelor’s degree and 1-3 years of experience in a GMP-regulated environment. This contract position offers benefits such as medical insurance and a 401(k).

Qualifications

• 1–3+ years of experience in a GMP-regulated environment, preferably in Pharma or Biotech.
• Working knowledge of cGMP and regulatory guidelines.

Responsibilities

• Review and approve GMP documents, including SOPs, specifications, and batch records.
• Perform batch record reviews and support product release activities.
• Support deviation, CAPA, investigation, and change control processes.

Skills

Attention to detail

Communication skills

Education

Bachelor’s degree in a scientific or related field

Job description

Base pay range

$35.00/hr - $50.00/hr

Job Title

Scientific & Technical Recruiter @ Astrix | Driving Innovation by Connecting Top Talent with Leading Life Science Companies

Position: QA Associate II/III

Job Type

Contract until January 2026 (possibility of extension)

Summary: We are seeking a QA Associate to support quality operations within our manufacturing facility. This role ensures compliance with cGMP requirements, supports batch release activities, and provides QA oversight for day-to-day production operations.

Our client is a global player in the biotech field, primarily focusing on creating building blocks for advanced research and development, often supporting other companies in highly technical industries.

Key Responsibilities

• Review and approve GMP documents, including SOPs, specifications, and batch records.
• Perform batch record reviews and support product release activities.
• Support deviation, CAPA, investigation, and change control processes.
• Provide on-the-floor QA oversight (line clearance, material verification, compliance checks).
• Assist with internal and external audits and regulatory inspections.
• Support validation and qualification activities (equipment, processes, cleaning).
• Maintain QA logs, training records, and document control systems.

Qualifications

• Bachelor’s degree in a scientific or related field.
• 1–3+ years of experience in a GMP-regulated environment (Pharma or Biotech preferred).
• Working knowledge of cGMP and regulatory guidelines.
• Strong attention to detail and excellent communication skills.

This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Seniority level

Mid-Senior level

Employment type

Contract

Job function

Quality Assurance

Benefits

• Medical insurance
• 401(k)
• Vision insurance